Key result
Apixaban resulted in a significantly higher 12-month venous patency rate (80.5%) compared to vitamin K antagonists (68%) in patients with acute iliofemoral deep vein thrombosis treated with pharmaco-mechanical catheter-directed thrombolysis.
Why the study?
The comparative pharmacologic stability, recurrent venous thromboembolism, major bleeding, and net clinical benefit of VKA, LMWH, and DOAC regimens for long-term anticoagulation after PMCDT for DVT were unclear.
Does apixaban improve patency, reduce complications, and offer better clinical benefit compared to LMWH or VKA in patients with acute iliofemoral DVT treated with PMCDT?
Cohort (n=225)
No
Does apixaban improve patency, reduce complications, and offer better clinical benefit compared to LMWH or VKA in patients with acute iliofemoral DVT treated with PMCDT?
Apixaban provides a safe and effective alternative to VKA and LMWH for long-term anticoagulation after PMCDT in acute DVT, offering better patency, compliance, and quality of life.
May support apixaban over VKA post-PM-CDT in iliofemoral DVT; hypothesis-generating and leaves open need for RCTs.
Aim: We aimed to compare the stability of pharmacologic profile, rate of symptomatic recurrent venous thromboembolism, major bleeding and the net clinical benefit on the regimen with vitamin K antagonist (VKA), low molecular weight heparin (LMWH) and direct oral anticoagulant (DOAC) for long-term anticoagulation in patients undergoing pharmaco-mechanical catheter-directed thrombolysis (PMCDT) for the treatment of deep vein thrombosis (DVT). Material and Methods: During the period from January 2019 until June 2019, data of 112 patients who underwent PMCDT for the treatment of acute iliofemoral DVT in our institution with long-term apixaban (Pfizer, Turkey) medication were prospectively collected (Group 1-DOAC). Data of control groups within January 2017- December 2018 period were collected retrospectively. Control groups consisted of PMCDT patients with extended LMWH (Tinzaparin, Abdi Ibrahim Pharma, Turkey) treatment (Group 2-LMWH; N=119) and with VKA (Coumadin, Eczacibasi Pharma, Turkey) treatment (Group 3- Control; N=111). Results: Patients treated with VKA showed a significant incompliance starting from third month up to one year. Patency rate diminished significantly below 70%. 32% of VKA patients were out of therapeutic range even in the first month leading to 40% at the end of the year. Likert Scale, Villalta/VCCS and VEINES-QOL-Sym scores confirmed the clinical data. Conclusion: This study highlights the potential role of DOAC as a reasonable alternative to VKAs/LMWH in the long-term anticoagulation strategy for DVT. We await larger clinical trials to support these findings and establish the role of DOAC as the standard of care for patients with DVT.
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Günaydın et al. (2020) conducted a cohort in Acute iliofemoral deep vein thrombosis (n=225). Apixaban vs. Vitamin K antagonists or Low molecular weight heparin was evaluated on Venous patency rate at 12 months (p=<0.05). Apixaban resulted in a significantly higher 12-month venous patency rate (80.5%) compared to vitamin K antagonists (68%) in patients with acute iliofemoral deep vein thrombosis treated with pharmaco-mechanical catheter-directed thrombolysis.
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